Ian M Campbell

9PUBLICATIONS
52CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Genetic immunologyHuman biophysicsDecision support and group support systemsPeripheral nervous system
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Publications (9)

|Mar 23, 2026
Interpretable Fine-tuned Large Language Models Facilitate Making Genetic Test Decisions for Rare Diseases.

Quan M Nguyen, Fangyi Chen, Cong Liu

|Apr 03, 2024
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia.

Katherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu

|Oct 31, 2023
PhenoID, a language model normalizer of physical examinations from genetics clinical notes.

Davy Weissenbacher, Siddharth Rawal, Xinwei Zhao

|Apr 20, 2023
Clinical decision support with a comprehensive in-EHR patient tracking system improves genetic testing follow up.

Ian M Campbell, Dean J Karavite, Morgan L Mcmanus

|Jul 21, 2021
Provider Perspectives on the Impact of the COVID-19 Pandemic on Newborn Screening.

Jessica I Gold, Ian M Campbell, Can Ficicioglu

|Mar 30, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.

Sarah E Sheppard, Ian M Campbell, Margaret H Harr

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Frequent Collaborators

2 joint publications

Sarah E Sheppard

2 joint publications

Katherine M Szigety

1 joint publications

T Blaine Crowley

1 joint publications

Marta Unolt